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Articolul urmator |
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Ultima descărcare din IBN: 2024-03-20 22:39 |
SM ISO690:2012 COSTIUC, Ecaterina, BERNIC, Jana, LISIŢA, Natalia. Nefroblastomul la copii. Prezentare de cazuri clinice. In: Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, 21-23 octombrie 2020, Chişinău. Chişinău: USMF, 2020, p. 614. |
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Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” 2020 | ||||||
Congresul "Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”" Chişinău, Moldova, 21-23 octombrie 2020 | ||||||
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Pag. 614-614 | ||||||
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Nephroblastoma accounts for 85% of all kidney tumors in children, and only 6% of all tumors in children. Most cases are sporadic and only 2% are genetically transmitted. Up to 5% have a bilateral location. The maximum incidence of tumor detection is at the age of 3-4 years. Objective of the study. Attracting the attention of doctors, especially urologists on the possible manifestation of nephroblastoma, to the first degree relatives of the patient, in whom up to a certain point the pathology can be practically asymptomatic. Material and Methods. Analysis of clinical cases of 2 sisters hospitalized in the urological service, Natalia Gheorghiu NSPC for Pediatric Surgery, PHI IMC. The first patient (2 years and 8 months) with a right kidney tumor. The second (3 years and 11 months) - with tumor damage of both kidneys with an insidious onset and asymmetry of the abdominal wall. Both diagnosed on routine ultrasound, confirmed on CT. Results. Surgical solution in the first patient - nephrectomy on the right; in the second - subtotal removal of tumors by laparoscopic approach with preservation of the kidneys. The histopathological conclusion of the removed pieces in both patients was the same: interlobulated blastemoepithelial nephroblastoma. Adjuvant treatment was extended in the PHI Institute of Oncology. Two years after the surgery, the condition of the first patient is satisfactory; in the second patient nephrolithiasis developed as a result of kidney deformity after surgery. Conclusion. The analysis of these clinical cases demonstrates the presence of hereditary factor in the occurrence of nephroblastoma in these two sisters, which requires routine renal ultrasound in first-degree relatives of patients diagnosed with nephroblastoma. |
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Cuvinte-cheie kidney tumors in children, Nephroblastoma, Wilms tumor, tumori renale la copii, nefroblastom, tumora Wilms |
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